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10.1038/ni.3632

http://scihub22266oqcxt.onion/10.1038/ni.3632
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C5164931!5164931!27893700
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suck abstract from ncbi


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pmid27893700      Nat+Immunol 2017 ; 18 (1): 74-85
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  • Trans-presentation of interleukin-6 by dendritic cells is required for priming pathogenic TH17 cells #MMPMID27893700
  • Heink S; Yogev N; Garbers C; Herwerth M; Aly L; Gasperi C; Husterer V; Croxford AL; Möller-Hackbarth K; Bartsch HS; Sotlar K; Krebs S; Regen T; Blum H; Hemmer B; Misgeld T; Wunderlich TF; Hidalgo J; Oukka M; Rose-John S; Schmidt-Supprian M; Waisman A; Korn T
  • Nat Immunol 2017[Jan]; 18 (1): 74-85 PMID27893700show ga
  • The cellular sources of interleukin-6 (IL-6) that are relevant for the differentiation of TH17 cells remain unclear. Here, we used a novel strategy of IL-6 conditional deletion of distinct IL-6-producing cell types to show that Sirp?+ dendritic cells (DC) were essential for the generation of pathogenic TH17 cells. During the process of cognate interaction, Sirp?+ DCs trans-presented IL-6 to T cells using their own IL-6R?. While ambient IL-6 was sufficient to suppress the induction of the transcription factor Foxp3 in T cells, IL-6 trans-presentation by DC-bound IL-6R? (here defined as IL-6 cluster signaling) was required to prevent premature induction of IFN-? in T cells and to generate pathogenic TH17 cells in vivo. These findings will guide therapeutic approaches for TH17-mediated autoimmune diseases.
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